Adenovirus-mediated gene transfer into tendon and tendon sheath

被引:72
作者
Lou, J
Manske, PR
Aoki, M
Joyce, ME
机构
[1] Department of Orthopaedic Surgery, 11300 West Pavilion, Washington University Medical School, St. Louis, MO 63110, One Barnes Hospital Plaza
关键词
GROWTH-FACTORS; EXPRESSION;
D O I
10.1002/jor.1100140403
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
In this study, we successfully transferred the Escherichia coli beta-galactosidase gene, LacZ, into the chicken tendon and tendon sheath by a recombinant adenovirus. The recombinant adenovirus Adv-beta gal that carried the E. coli LacZ gene was constructed by homologous recombination in 293 cells (human transformed embryonic kidney) between the expressing vector and the ClaI large fragment of adenovirus 5 genome. Each chicken received a 10 mu l injection, containing 10(5) plaque-forming units of recombinant virus Adv-beta gal, into the tendon sheath of the long toe, Samples of tendon and tendon sheath were harvested at 3, 30, and 75 days after the injection, The LacZ gene transfer was detected for its coding product beta-galactosidase by staining with X-gal solution. The results showed that all tendon and tendon sheath samples from the three harvest times stained positive (blue). The tendon sheath samples were more extensively stained; staining of the tendon was limited to the epitenon layer. These data suggest that a functional exogenous gene can potentially be transferred into the tendon and tendon sheath by similar techniques; such techniques may be used to improve healing and reduce adhesion formation.
引用
收藏
页码:513 / 517
页数:5
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